Create and execute complex regulatory implementation strategies for assigned legislative, regulatory, sub-regulatory, and licensing / accreditation requirements across multiple jurisdictions, including assessments of the regulatory impact of changes to people, processes, and technologies deployed ac...
The Electric Pricing and Customer Program (EPCP) Branch within the Public Advocates Office is seeking a Public Utilities Regulatory Analyst IV-V to join its Customer Programs team. As a senior analyst, the incumbent will take a lead role in research and analysis on a variety of building decarbonizat...
Individuals interested in applying for this vacancy must have eligibility.If you are new to state service or need to gain eligibility to these classifications, please click or to open the examination bulletin and follow the instructions on “How to apply”.The examination is a separate process from ap...
The analyst will make recommendations based on independent analysis of regulatory, policy and technical issues. Under general direction of the Project and Program Supervisor, the analyst will support the Electric Market Design Section in the development of work products that are used to advise and a...
We have an opportunity to join the Alliance as a Provider Data Analyst II in the Operations Management Department. Performs data analysis and research to support provider data management strategies. Data transmission, provider file formats, such as 274, provider rosters, provider directories, HIPAA,...
When you join Design Group as a Project Manager, you are joining a team that will challenge you and position you for growth. Manage project tasks including hardware and panel design, PLC and HMI programming, SCADA design, power distribution design, and all associated project documentation. Manage pr...
The Regulatory Specialist is a part of Research and Development, this team is responsible for assessing ingredient safety and regulatory compliance, coordinating safety, micro, stability, compatibility and claims testing, ensuring product compliance with international cosmetic regulations, and advis...
Regional Compliance Specialist. Assist in turning around low-performing divisions' compliance numbers and contribute to the continuous improvement of the company’s compliance program and processes. In collaboration with Region Safety Directors, GMs, and division safety, develop and implement strateg...
Utilize MS Project and other project management tools to monitor project budgets and timelines, ensuring projects are delivered on time and within budget. We seek an experienced Senior HVAC Project Manager to oversee large-scale commercial HVAC projects in Orange, CA. Job Title: Senior HVAC Project ...
Environmental Permitting and Compliance Specialist). Environmental Permitting and Compliance Specialist). Join Yorke Engineering, LLC, an Environmental Consulting leader in California that implements Environmental Engineering and Compliance solutions for our clients throughout California. Our missio...
Project Managers (levels I, II, and/or III). Licensed professional or Certified Construction Manager (CCM) or PMP. Work experience in project planning and development. Ability to independently manage all aspects of a project. ...
Perform on-site Project Manager duties on small scope projects. Multi-Family Construction/Development Group currently seeking a Project Manager. Provide direction to the project team to complete the projects safe and on time. Work with preconstruction, estimating and scheduling on project estimate a...
We are currently seeking a Senior Regulatory Affairs Specialist to drive regulatory strategies and submissions for medical devices. Senior Regulatory Affairs Specialist. Hands-on experience with major regulatory submissions and managing interactions with regulatory agencies. Develop and implement gl...
Senior Regulatory Affairs Specialist. Draft, edit, and compile technical documentation and design dossiers to support CE mark/UKCA mark regulatory filings. Prepare regulatory submissions for FDA 510(k) clearance and A2F submissions. Research regulatory requirements from FDA, CMDR, MDR, IVDR, and UK ...
Collaborate with data managers, statistical programmers, biostatistics, clinical operations, and external vendors to review, sign off on the data transfer specifications, and transfer data from external sources, ensuring data is received and validated for data integrity. Work with data managers and ...
Senior/Principal Regulatory Specialist (Hybrid). Lead regulatory strategy and submissions (PMA, IDE) for Class III medical devices. Support global regulatory registrations and maintain compliance. ...
We are seeking a Principal Regulatory Affairs Specialist to support regulatory strategies and submissions for Class III medical devices. Lead regulatory submissions for Class III devices and maintain regulatory communications. This role will involve collaborating with cross-functional teams, contrib...
The Ideal candidate will have 3 years of experience as a Business Analyst within D365 FO and is looking for someone to work Hybr. ...
BI Analyst - Proficiency in SQL, including advanced querying techniques, data manipulation, and performance optimization - Strong experience with ETL tools and processes, including SQLSSIS, Python, or other data transformation tools - Proficiency with databases and data warehouses (e. A large health...
Joby Aviation is seeking a Senior Facilities Project Portfolio Manager to oversee the varied and complex array of facilities projects necessary to build out our facilities in California. Create and manage an enterprise level, multi-project facilities project portfolio including oversight of schedule...
A medical device client of ours in the East Bay Area is looking to bring on a Regulatory Affairs Specialist IV position!. Years of Regulatory Affairs experience across the medical device space. International Regulatory Affairs Experience Required (Europe specifically). ...
This is a general application for compliance professionals in the life sciences sector. ...
Chief Compliance Officer (San Francisco, CA): Our client, a successful hedge fund with approximately $3B in AUM, is seeking a talented and experienced CCO to help run all aspects of the compliance program. Manage the firm’s overall compliance program and develop, review, and update the firm's compli...
Compliance & Ethics Specialist. Perform field and desk monitoring to ensure compliance with to relevant laws and regulations. Track, analyze, and report on compliance monitoring progress, identifying trends and potential risks. Provide compliance guidance and support for various initiatives and proj...
A degree in a life science, chemistry, or chemical engineering or closely related discipline with a graduate degree preferred and at least 10 years of experience in pharmaceutical regulatory affairs, that includes, but cannot be limited to, CMC regulatory affairs. Associate) Director, Regulatory Aff...